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2. Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome. Niessen RC; Hofstra RM; Westers H; Ligtenberg MJ; Kooi K; Jager PO; de Groote ML; Dijkhuizen T; Olderode-Berends MJ; Hollema H; Kleibeuker JH; Sijmons RH Genes Chromosomes Cancer; 2009 Aug; 48(8):737-44. PubMed ID: 19455606 [TBL] [Abstract][Full Text] [Related]
3. Frequency of rearrangements in Lynch syndrome cases associated with MSH2: characterization of a new deletion involving both EPCAM and the 5' part of MSH2. Pérez-Cabornero L; Infante Sanz M; Velasco Sampedro E; Lastra Aras E; Acedo Becares A; Miner Pino C; Durán Domínguez M Cancer Prev Res (Phila); 2011 Oct; 4(10):1556-62. PubMed ID: 21791569 [TBL] [Abstract][Full Text] [Related]
4. Identification of a founder EPCAM deletion in Spanish Lynch syndrome families. Mur P; Pineda M; Romero A; Del Valle J; Borràs E; Canal A; Navarro M; Brunet J; Rueda D; Ramón Y Cajal T; Lázaro C; Caldés T; Blanco I; Soto JL; Capellá G Clin Genet; 2014 Mar; 85(3):260-6. PubMed ID: 23530899 [TBL] [Abstract][Full Text] [Related]
5. EPCAM germline and somatic rearrangements in Lynch syndrome: identification of a novel 3'EPCAM deletion. Spaepen M; Neven E; Sagaert X; De Hertogh G; Beert E; Wimmer K; Matthijs G; Legius E; Brems H Genes Chromosomes Cancer; 2013 Sep; 52(9):845-54. PubMed ID: 23801599 [TBL] [Abstract][Full Text] [Related]
6. Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases. Rumilla K; Schowalter KV; Lindor NM; Thomas BC; Mensink KA; Gallinger S; Holter S; Newcomb PA; Potter JD; Jenkins MA; Hopper JL; Long TI; Weisenberger DJ; Haile RW; Casey G; Laird PW; Le Marchand L; Thibodeau SN J Mol Diagn; 2011 Jan; 13(1):93-9. PubMed ID: 21227399 [TBL] [Abstract][Full Text] [Related]
7. Usefulness of epithelial cell adhesion molecule expression in the algorithmic approach to Lynch syndrome identification. Musulen E; Blanco I; Carrato C; Fernandez-Figueras MT; Pineda M; Capella G; Ariza A Hum Pathol; 2013 Mar; 44(3):412-6. PubMed ID: 23026194 [TBL] [Abstract][Full Text] [Related]
8. Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis. Vargas-Parra GM; González-Acosta M; Thompson BA; Gómez C; Fernández A; Dámaso E; Pons T; Morak M; Del Valle J; Iglesias S; Velasco À; Solanes A; Sanjuan X; Padilla N; de la Cruz X; Valencia A; Holinski-Feder E; Brunet J; Feliubadaló L; Lázaro C; Navarro M; Pineda M; Capellá G Int J Cancer; 2017 Oct; 141(7):1365-1380. PubMed ID: 28577310 [TBL] [Abstract][Full Text] [Related]
9. Recurrence and variability of germline EPCAM deletions in Lynch syndrome. Kuiper RP; Vissers LE; Venkatachalam R; Bodmer D; Hoenselaar E; Goossens M; Haufe A; Kamping E; Niessen RC; Hogervorst FB; Gille JJ; Redeker B; Tops CM; van Gijn ME; van den Ouweland AM; Rahner N; Steinke V; Kahl P; Holinski-Feder E; Morak M; Kloor M; Stemmler S; Betz B; Hutter P; Bunyan DJ; Syngal S; Culver JO; Graham T; Chan TL; Nagtegaal ID; van Krieken JH; Schackert HK; Hoogerbrugge N; van Kessel AG; Ligtenberg MJ Hum Mutat; 2011 Apr; 32(4):407-14. PubMed ID: 21309036 [TBL] [Abstract][Full Text] [Related]
10. Lynch syndrome-associated extracolonic tumors are rare in two extended families with the same EPCAM deletion. Lynch HT; Riegert-Johnson DL; Snyder C; Lynch JF; Hagenkord J; Boland CR; Rhees J; Thibodeau SN; Boardman LA; Davies J; Kuiper RP; Hoogerbrugge N; Ligtenberg MJ Am J Gastroenterol; 2011 Oct; 106(10):1829-36. PubMed ID: 21769135 [TBL] [Abstract][Full Text] [Related]
11. Screening for germline mutations of MLH1, MSH2, MSH6 and PMS2 genes in Slovenian colorectal cancer patients: implications for a population specific detection strategy of Lynch syndrome. Berginc G; Bracko M; Ravnik-Glavac M; Glavac D Fam Cancer; 2009; 8(4):421-9. PubMed ID: 19526325 [TBL] [Abstract][Full Text] [Related]
12. Novel MLH1 duplication identified in Colombian families with Lynch syndrome. Alonso-Espinaco V; Giráldez MD; Trujillo C; van der Klift H; Muñoz J; Balaguer F; Ocaña T; Madrigal I; Jones AM; Echeverry MM; Velez A; Tomlinson I; Milà M; Wijnen J; Carvajal-Carmona L; Castells A; Castellví-Bel S Genet Med; 2011 Feb; 13(2):155-60. PubMed ID: 21233718 [TBL] [Abstract][Full Text] [Related]
14. Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome. Schneider NB; Pastor T; Paula AE; Achatz MI; Santos ÂRD; Vianna FSL; Rosset C; Pinheiro M; Ashton-Prolla P; Moreira MÂM; Palmero EI; Cancer Med; 2018 May; 7(5):2078-2088. PubMed ID: 29575718 [TBL] [Abstract][Full Text] [Related]
15. Identification of a Japanese Lynch syndrome patient with large deletion in the 3' region of the EPCAM gene. Eguchi H; Kumamoto K; Suzuki O; Kohda M; Tada Y; Okazaki Y; Ishida H Jpn J Clin Oncol; 2016 Feb; 46(2):178-84. PubMed ID: 26613680 [TBL] [Abstract][Full Text] [Related]
16. Universal screening for Lynch syndrome in endometrial cancers: frequency of germline mutations and identification of patients with Lynch-like syndrome. Dillon JL; Gonzalez JL; DeMars L; Bloch KJ; Tafe LJ Hum Pathol; 2017 Dec; 70():121-128. PubMed ID: 29107668 [TBL] [Abstract][Full Text] [Related]
17. Analysis of EPCAM protein expression in diagnostics of Lynch syndrome. Kloor M; Voigt AY; Schackert HK; Schirmacher P; von Knebel Doeberitz M; Bläker H J Clin Oncol; 2011 Jan; 29(2):223-7. PubMed ID: 21115857 [TBL] [Abstract][Full Text] [Related]
18. The molecular basis of EPCAM expression loss in Lynch syndrome-associated tumors. Huth C; Kloor M; Voigt AY; Bozukova G; Evers C; Gaspar H; Tariverdian M; Schirmacher P; von Knebel Doeberitz M; Bläker H Mod Pathol; 2012 Jun; 25(6):911-6. PubMed ID: 22388758 [TBL] [Abstract][Full Text] [Related]
19. Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. Lagerstedt-Robinson K; Rohlin A; Aravidis C; Melin B; Nordling M; Stenmark-Askmalm M; Lindblom A; Nilbert M Oncol Rep; 2016 Nov; 36(5):2823-2835. PubMed ID: 27601186 [TBL] [Abstract][Full Text] [Related]
20. Prevalence of mismatch repair-deficient crypt foci in Lynch syndrome: a pathological study. Kloor M; Huth C; Voigt AY; Benner A; Schirmacher P; von Knebel Doeberitz M; Bläker H Lancet Oncol; 2012 Jun; 13(6):598-606. PubMed ID: 22552011 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]